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CoRoent 6080823Recalls & reported problems

Nuvasive, Inc. · CoRoent® Large MP, 8x9x23 8° · Class 2 · Implant

All models of CoRoent (64)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517283405), received between Mar 30, 2016 and Mar 30, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1
  • Mechanical Problem1
  • Unintended Movement1

Patient problems

  • Failure of Implant1
  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 30, 2016Mechanical Problem; Device Dislodged or Dislocated; Unintended Movement; Mechanical Problem; Device Dislodged or Dislocated; Unintended Movement

    ON (B)(6) 2015 A (B)(6) MALE HAD AN INTERVERTEBRAL FUSION DEVICE PLACED AT L5-1. THE CAGE LOOKS TO HAVE MIGRATED POSTERIORLY INTO THE VERTEBRAL FORAMEN. PATIENT REPORTED PAIN, BUT DID NOT SUSTAIN A FALL OR INJURY. THE SURGEON HAS ELECTED TO MONITOR THE PATIENT. NO REVISION SURGERY HAS BEEN SCHEDULED AT THIS TIME.

    Patient problems: Failure of Implant; Pain

    MAUDE report 5536769 ↗

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Sources and updates

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